...
首页> 外文期刊>Journal of Materials Science >Single step electrochemical synthesis of Sb_2Se_3 thin films: Effect of molarities of precursor solution
【24h】

Single step electrochemical synthesis of Sb_2Se_3 thin films: Effect of molarities of precursor solution

机译:单步电化学合成Sb_2Se_3薄膜:前驱体溶液摩尔浓度的影响

获取原文
获取原文并翻译 | 示例

摘要

In the present investigation, we have successfully synthesized polycrystalline Sb_2Se_3 thin films by single-step electrochemical method. Effect of concentration of precursor solution on structural, morphological, optical, and wettability properties by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), optical absorption, and contact angle measurement have been investigated. It is evident from XRD pattern that Sb_2Se_3 thin films are polycrystalline having orthorhombic crystal structure. Also, as precursor concentration increases the diffraction peak intensity also increases. Scanning electron micrographs reveal that the increase in precursor concentration causes the formation of soap foam like microstructure which is spread in the form of ellipsoids over whole substrate surface. The optical band gap decreases from 1.49 to 1.35 eV and contact angle decreases from 40° to 13°, i.e., the surface of Sb _2Se_3 thin films converts from hydrophilic to superhydrophilic nature due to increase in precursor concentration. In addition, the holographic interferometric properties have been studied. The thickness, stress to substrate and deposited mass of the thin films is determined using double exposure holographic interferometry (DEHI) technique.
机译:在本研究中,我们已经成功地通过单步电化学方法合成了多晶Sb_2Se_3薄膜。通过X射线衍射(XRD),扫描电子显微镜(SEM),光吸收和接触角测量研究了前体溶液浓度对结构,形态,光学和润湿性的影响。从XRD图案可以明显看出,Sb_2Se_3薄膜是具有正交晶体结构的多晶。另外,随着前驱物浓度的增加,衍射峰强度也增加。扫描电子显微照片显示,前体浓度的增加导致形成类似整体结构以椭圆体形式散布的肥皂泡沫状微观结构。光学带隙从1.49 eV降低到1.35 eV,接触角从40°降低到13°,即Sb _2Se_3薄膜的表面由于前驱物浓度的增加而从亲水性转变为超亲水性。另外,已经研究了全息干涉测量特性。薄膜的厚度,对衬底的应力和沉积质量是使用两次曝光全息干涉法(DEHI)技术确定的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号